Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 19:41966116 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.41966116G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays